HR c.3233G>C ;(p.G1078A)

Variant ID: 8-21974533-C-G

NM_005144.4(HR):c.3233G>C;(p.G1078A)

This variant was identified in 1 publication

View GRCh38 version.



Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP

Publications:

Influence of CYP2C9 and VKORC1 1173C/T genotype on the risk of hemorrhagic complications in African-American and European-American patients on warfarin.

Clinical Pharmacology And Therapeutics
Limdi, N A NA; McGwin, G G; Goldstein, J A JA; Beasley, T M TM; Arnett, D K DK; Adler, B K BK; Baird, M F MF; Acton, R T RT
Publication Date: 2008-02

Variant appearance in text: HR: G1078A
PubMed Link: 17653141
Variant Present in the following documents:
  • Main text
View BVdb publication page